Lifeline Medical Devices Pvt. Ltd.

a) The conformity of the devices shall be appropriately checked, as per the QMS requirement. b) Keeping Technical Documents and EC Declaration of conformity up to date. C) Continuously monitor the Postmarket activities of medical devices, d) Reporting Analysis of Serious Incidents, Field safety corrective actions (FSCA), Analysis of Vigilance and Trend reporting.

• a) The conformity of the devices shall be appropriately checked, as per the QMS requirement. b) Keeping Technical Documents and EC Declaration of conformity up to date. C) Continuously monitor the Postmarket activities of medical devices, d) Reporting Analysis of Serious Incidents, Field safety corrective actions (FSCA), Analysis of Vigilance and Trend reporting.